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Astral Medical Systems

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900506MODIFIED COATRON II AND COATRON JR.March 12, 1990
K851153COATRON F(SAME AS COATRON, BUT ALSO DOES FIBRINOGENovember 5, 1985
K853734APOLLO DENSITOMETERSeptember 25, 1985
K851154ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18May 13, 1985